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Image Search Results
Journal: bioRxiv
Article Title: Identification of a lineage-agnostic splicing signature caused by PRMT5 inhibition
doi: 10.64898/2026.03.26.714409
Figure Lengend Snippet: A: Determination of maximum effect (Amax) in 34 cancer cell lines representing multiple cancer lineages including melanoma, pancreatic adenocarcinoma, mesothelioma, non-small cell carcinoma, cholangiocarcinoma, and glioblastoma following 7-days TNG908 treatment. Cell lines are colored by MTAP status. B: Exemplar SDMA immunoblot following a 3-day treatment with TNG908 at cell line-specific EC 20 and EC 50 concentrations from . C: PRMT5 and MTAP levels of cell lines from . D: Correlation of normalized PRMT5 (left) or a single SDMA-modified substrate (right) immunoblot levels at the cell line-specific EC 50 . E: PRMT5 and SDMA immunoblots following treatment a 3-day treatment of TNG908 at 0.02, 0.08, 0.31, 1.25, 5µM in MTAP -deleted LN18 cells.
Article Snippet: Human cancer cell lines: skin cutaneous melanoma (SK-MEL-5, A101D, Hs294T, IGR-1, SH-4), glioblastoma (LN18, GB-1, U-87 MG, AM-38, KS-1, A172), pancreatic adenocarcinoma (Panc03.27, Panc10.05, SU.86.86, BxPC-3, Miapaca2), mesothelioma (ONE58, SDM103T2, NCI-H2052, ZL5, ACC-MESO-4), cholangiocarcinoma (KKU-100),
Techniques: Western Blot, Modification
Journal: bioRxiv
Article Title: Identification of a lineage-agnostic splicing signature caused by PRMT5 inhibition
doi: 10.64898/2026.03.26.714409
Figure Lengend Snippet: A: Heatmap of 22 distinct alternative splicing events (ASE) following 3-days TNG908 treatment in the MTAP -deleted GBM LN-18 cell line. Data reported as percent spliced in (PSI) of the alternative exons (% inclusion = inclusion/sum of inclusion + exclusion). Table of PSI values transformed, plotted, and expressed as LogIC 50 values. B: Heatmap of 22 ASEs expressed as PSI following 3-day treatment of 1µM TNG908 in LN-18 MTAP -WT or LN-18 MTAP -deleted cells. C: Heatmap of 22 distinct ASEs from MTAP -deleted cells treated for 3-days with treated with 1µM TNG908, the maximally efficacious dose identified from Figure 2.1. Data reported as ΔPSI of the alternative exons (ΔPSI = PSI DMSO – PSI TNG908). Cell lines represent glioblastoma (GBM), colorectal cancer (CRC), non-small cell lung cancer (NSCLC), and pancreatic adenocarcinoma (PDAC). D: ΔPSI of RPAIN ASE for treated cell lines.
Article Snippet: Human cancer cell lines: skin cutaneous melanoma (SK-MEL-5, A101D, Hs294T, IGR-1, SH-4), glioblastoma (LN18, GB-1, U-87 MG, AM-38, KS-1, A172), pancreatic adenocarcinoma (Panc03.27, Panc10.05, SU.86.86, BxPC-3, Miapaca2), mesothelioma (ONE58, SDM103T2, NCI-H2052, ZL5, ACC-MESO-4), cholangiocarcinoma (KKU-100),
Techniques: Alternative Splicing, Transformation Assay
Journal: bioRxiv
Article Title: Identification of a lineage-agnostic splicing signature caused by PRMT5 inhibition
doi: 10.64898/2026.03.26.714409
Figure Lengend Snippet: A: Determination of maximum effect (Amax) in 34 cancer cell lines representing multiple cancer lineages including melanoma, pancreatic adenocarcinoma, mesothelioma, NSCLC, cholangiocarcinoma, and glioblastoma following 7-days TNG908 treatment. Cell lines are colored by MTAP status. B: Normalized SDMA levels following a 1-day exogenous administration of MTA in HAP1 MTAP -WT cells.
Article Snippet: Human cancer cell lines: skin cutaneous melanoma (SK-MEL-5, A101D, Hs294T, IGR-1, SH-4), glioblastoma (LN18, GB-1, U-87 MG, AM-38, KS-1, A172), pancreatic adenocarcinoma (Panc03.27, Panc10.05, SU.86.86, BxPC-3, Miapaca2), mesothelioma (ONE58, SDM103T2, NCI-H2052, ZL5, ACC-MESO-4), cholangiocarcinoma (KKU-100),
Techniques:
Journal: bioRxiv
Article Title: Loss of the endocytic tumor suppressor HD-PTP phenocopies LKB1 and promotes RAS-driven oncogenesis
doi: 10.1101/2023.01.26.525772
Figure Lengend Snippet: A) Western blot of indicated signaling proteins in SW1573 (KRAS G12C /LKB1 WT ) and H1299 (NRAS Q61K /LKB1 WT ) lung cancer cells expressing either scrambled control, HD-PTPshRNA or HD-PTP siRNA. B) Brightfield images of 2D invasion assays of SW1573 and H1299 cells expressing scrambled control and shRNA or siRNA to HD-PTP. C) Growth of cell populations expressing either shRNA or siRNA to HD-PTP. D) Quantitation of invading cells from 2D invasion assays in (B). 2D invasion assays were performed using three biological replicates. Error bars represent the Std. Deviation of Mean. Statistical significance was analyzed using the student’s t-test. * = <.05; ** = <.01. E) Representative images of SW1573 3D spheroids expressing either scrambled control or HD-PTP shRNA and embedded in invasion matrix for the indicated time. Quantification of invasive area in the SW1573 assay in (E). G) Representative images of H1299 spheroids expressing scrambled control or siRNA to HD-PTP and embedded in invasion matrix for the indicated time. H) Quantification of invasive area in the H1299 invasion assay in (G). Quantification of invasive area in H1299 (I) and SW1573 (J) cells expressing scrambled control or shRNA to HD-PTP and treated with vehicle control (DMSO) or the FAK inhibitor defactinib. Quantitative data were analyzed using 4-5 biological replicates. Error bars represent Std. Deviation of Mean and statistical significance was tested using one-way ANOVA, multiple comparisons. * = <.05; ** = <.01; **** = <.0001.
Article Snippet:
Techniques: Western Blot, Expressing, Control, shRNA, Quantitation Assay, Invasion Assay